Homo sapiens (human): 10975
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Entry
10975 CDS
T01001
Symbol
UQCR11, 0710008D09Rik, QCR10, UQCR
Name
(RefSeq) ubiquinol-cytochrome c reductase, complex III subunit XI
KO
K00420
ubiquinol-cytochrome c reductase subunit 10
Organism
hsa
Homo sapiens (human)
Pathway
hsa00190
Oxidative phosphorylation
hsa01100
Metabolic pathways
hsa04260
Cardiac muscle contraction
hsa04714
Thermogenesis
hsa04932
Non-alcoholic fatty liver disease
hsa05010
Alzheimer disease
hsa05012
Parkinson disease
hsa05014
Amyotrophic lateral sclerosis
hsa05016
Huntington disease
hsa05020
Prion disease
hsa05022
Pathways of neurodegeneration - multiple diseases
hsa05208
Chemical carcinogenesis - reactive oxygen species
hsa05415
Diabetic cardiomyopathy
Module
hsa_M00152
Cytochrome bc1 complex
Network
nt06252
Mitochondrial ROS formation (cancer)
nt06461
Huntington disease
nt06463
Parkinson disease
nt06466
Pathways of neurodegeneration
Element
N00990
Electron transfer in Complex III
N00991
Mutation-caused aberrant Htt to electron transfer in Complex III
N01046
Maneb to electron transfer in Complex III
N01395
Cadmium to electron transfer in complex III
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09100 Metabolism
09102 Energy metabolism
00190 Oxidative phosphorylation
10975 (UQCR11)
09150 Organismal Systems
09153 Circulatory system
04260 Cardiac muscle contraction
10975 (UQCR11)
09159 Environmental adaptation
04714 Thermogenesis
10975 (UQCR11)
09160 Human Diseases
09161 Cancer: overview
05208 Chemical carcinogenesis - reactive oxygen species
10975 (UQCR11)
09164 Neurodegenerative disease
05010 Alzheimer disease
10975 (UQCR11)
05012 Parkinson disease
10975 (UQCR11)
05014 Amyotrophic lateral sclerosis
10975 (UQCR11)
05016 Huntington disease
10975 (UQCR11)
05020 Prion disease
10975 (UQCR11)
05022 Pathways of neurodegeneration - multiple diseases
10975 (UQCR11)
09166 Cardiovascular disease
05415 Diabetic cardiomyopathy
10975 (UQCR11)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
10975 (UQCR11)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
UCR_6-4kD
QCR10
Motif
Other DBs
NCBI-GeneID:
10975
NCBI-ProteinID:
NP_006821
OMIM:
609711
HGNC:
30862
Ensembl:
ENSG00000127540
Pharos:
O14957
(Tdark)
UniProt:
O14957
Structure
PDB
PDBj
LinkDB
All DBs
Position
19:complement(1597169..1605462)
Genome browser
AA seq
56 aa
AA seq
DB search
MVTRFLGPRYRELVKNWVPTAYTWGAVGAVGLVWATDWRLILDWVPYINGKFKKDN
NT seq
171 nt
NT seq
+upstream
nt +downstream
nt
atggtgacccggttcctgggcccacgctaccgggagctggtcaagaactgggtcccgacg
gcctacacatggggcgctgtgggcgccgtggggctggtgtgggccaccgattggcggctg
atcctggactgggtaccttacatcaatggcaagtttaagaaggataattaa
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integrated database retrieval system